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	1.	Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients. [electronic resource] by Brožková, Dana Šafka Posádka, Jan Laššuthová, Petra Mazanec, Radim Haberlová, Jana Sišková, Dana Sakmaryová, Iva Neupauerová, Jana Seeman, Pavel Producer: 20140528 In: Molecular medicine reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability. [electronic resource] by Zhang, Feng Seeman, Pavel Liu, Pengfei Weterman, Marian A J Gonzaga-Jauregui, Claudia Towne, Charles F Batish, Sat Dev De Vriendt, Els De Jonghe, Peter Rautenstrauss, Bernd Krause, Klaus-Henning Khajavi, Mehrdad Posadka, Jan Vandenberghe, Antoon Palau, Francesc Van Maldergem, Lionel Baas, Frank Timmerman, Vincent Lupski, James R Producer: 20100629 In: American journal of human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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